Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Jeneric/Pentron with 78 510(k) clearances. The most recent is a 510(k) clearance dated Apr 22, 2002: BOND-3 ADHESIVE.
| Apr 22, 2002 | BOND-3 ADHESIVEK020499 · KLE | 510(k) clearances |
| Feb 22, 2002 | BOND-1 C & BK013543 · KLE | 510(k) clearances |
| Feb 14, 2002 | DENTIN CONDITIONING AND ADHESIVE SYSTEM (BOND-1)K013542 · KLE | 510(k) clearances |
| Aug 23, 2001 | AVANTE MICRO CRYSTAL SYSTEMK012231 · EIH | 510(k) clearances |
| Aug 3, 2001 | FIRST FILL R.C.S.K011748 · KIF | 510(k) clearances |
| Jun 25, 2001 | QUELL DESENSITIZERK010957 · LBH | 510(k) clearances |
| Jun 22, 2001 | JP CAST 40K011331 · EJT | 510(k) clearances |
| Jun 22, 2001 | JP CAST 50K011330 · EJT | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
